Spironolactone-furosemide combination therapy and acid-base disorders in liver cirrhosis patients
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11130%2F20%3A10410742" target="_blank" >RIV/00216208:11130/20:10410742 - isvavai.cz</a>
Alternative codes found
RIV/00064203:_____/20:10410742 RIV/00023001:_____/20:00079637
Result on the web
<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=F7u3wW2B_M" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=F7u3wW2B_M</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.5414/CP203624" target="_blank" >10.5414/CP203624</a>
Alternative languages
Result language
angličtina
Original language name
Spironolactone-furosemide combination therapy and acid-base disorders in liver cirrhosis patients
Original language description
Objective: Respiratory alkalosis (RA) and dilutional hyperchloremic acidosis (DHA) are the most common acid-base balance (ABB) disorders in patients with liver cirrhosis. The aims of this study were to clarify whether RA develops in relation to DHA via respiratory compensation of metabolic acidosis and whether spironolactone in combination with low-dose furosemide - diuretics known to ameliorate DHA - positively affects RA in liver cirrhosis patients. Materials and methods: 59 patients with advanced cirrhosis were divided into two groups. Group D consisted of individuals (urine sodium concentration (UNa+) > 20 mmol/L) who responded to combination therapy consisting of spironolactone and low-dose furosemide. The non-D group consisted of individuals (UNa+ <= 20 mmol/L) who either did not respond to the treatment or who were not administered it. In both groups, we examined serum and urine concentrations of electrolytes and ABB parameters, including S-Na(+)-SCl- and S-Na(+)/SCl- values. Results: In group D, we found a statistically significant relationship between pCO(2) and SHCO3-: r = 0.756 (p < 0.001) and between pCO(2) and SNa+-SCl-: r = 0.522 (p = 0.001). Neither Salb nor the corrected anion gap were associated with changes in SHCO3- or pCO(2) values. Although SHCO3- values were normal, abnormal pCO(2) values were observed in one third of group D patients. Based on multivariable analysis, SHCO3- proved to be a statistically significant influencing factor on pCO(2) values. Conclusion: DHA contributes to the development of RA in individuals with liver cirrhosis. Reducing DHA by means of effective diuretic therapy comprising spironolactone and furosemide has a beneficial effect on RA in such patients.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
30104 - Pharmacology and pharmacy
Result continuities
Project
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Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2020
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
International Journal of Clinical Pharmacology and Therapeutics
ISSN
0946-1965
e-ISSN
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Volume of the periodical
58
Issue of the periodical within the volume
5
Country of publishing house
DE - GERMANY
Number of pages
7
Pages from-to
261-267
UT code for WoS article
000527343300003
EID of the result in the Scopus database
2-s2.0-85084167582